Reinhardt D, Ritter E, Butzheinen R, Schümann H J
Agents Actions. 1979 Jun;9(2):155-62. doi: 10.1007/BF02024727.
On guinea-pig ileum and rabbit mesenteric artery contracted by high potassium (100 mM) histamine produced relaxations which were inhibited by the H2-receptor antagonist metiamide. These results are thus indicative for the role of H2-receptors in mediating relaxation and for H1-receptors in mediating contraction on smooth muscle. Time course studies for the relaxing and cyclic AMP responses to histamine showed that the cyclic AMP increase preceded the H2-receptor mediated relaxation. The cyclic AMP increase in response to histamine was prevented by metiamide, but remained unaffected by mepyramine on both the guinea-pig ileum and the rabbit mesenteric artery. In addition, dose-response curves obtained on the mesenteric artery demonstrated that the H2-receptor mediated depressor responses coincided with cyclic AMP increases. Thus, these results gave clear-cut evidence that cyclic AMP is an intracellular metabolic event only implicit in the H2-receptor mediated relaxation, but not in the H1-receptor mediated contraction on smooth muscle preparations.
在由高钾(100 mM)收缩的豚鼠回肠和兔肠系膜动脉上,组胺可产生舒张作用,该作用被H2受体拮抗剂甲硫米特抑制。因此,这些结果表明H2受体在介导平滑肌舒张中起作用,而H1受体在介导平滑肌收缩中起作用。对组胺舒张反应和环磷酸腺苷(cAMP)反应的时程研究表明,cAMP增加先于H2受体介导的舒张。甲硫米特可阻止组胺引起的cAMP增加,但在豚鼠回肠和兔肠系膜动脉上,美吡拉敏对其均无影响。此外,在肠系膜动脉上获得的剂量反应曲线表明,H2受体介导的降压反应与cAMP增加一致。因此,这些结果提供了明确的证据,即cAMP是一种仅与H2受体介导的平滑肌舒张有关的细胞内代谢事件,而与H1受体介导的平滑肌收缩无关。